Figure 7
From: Recombinant anti-HIV MAP30, a ribosome inactivating protein: against plant virus and bacteriophage
The simultaneous inoculation of N. glutinosa seedling with purified TMV and transgenic total protein in three dilutions, and purified TMV plus rMAP30 in three dilutions. Purified TMV plus non-transgenic total protein (negative control) (Table 3). There were 16 replicates for each test. (a) Test conducted with undiluted transgenic total protein. (b) Test conducted with one second diluted transgenic total protein. (c) Test conducted with one-quarter dilution of transgenic total protein. (d) Test conducted with non-transgenic total protein in undiluted state. (e) Test conducted with undiluted rMAP30. (f) Test conducted with one second diluted rMAP30. (g) Test conducted with one-quarter dilution r MAP30. (h) Test conducted with non-transgenic total protein in undiluted state. D4 indicates the day of symptoms observation. The virus and buffer existed in the right half of each leaf, as well as the protein and virus within the left half of each leaf were inoculated. (i,j) The viral infection controlling graph for rMAP30 in different dilutions versus non-transgenic protein. The highest control percentage was observed when the undiluted rMAP30.
